2. Academic Validation
  3. Pharmacological and electrophysiological characterization of the novel Kv7 channel inhibitor racecadotril in Parkinson's disease

Pharmacological and electrophysiological characterization of the novel Kv7 channel inhibitor racecadotril in Parkinson's disease

  • Neuropharmacology. 2025 Jun 17:278:110565. doi: 10.1016/j.neuropharm.2025.110565.
Bo Yang 1,  Hui Liu 1,  Shifan Zhang 1,  Biao Liu 1,  Qiaoqiao Sun 1,  Wen Li 1,  Rong Zheng 1,  Qingzhuo Cui 1,  Yulin Gu 1,  Xiaoke Li 1,  Jie Zhang 2,  Yidong Liu 3,  Fan Zhang 4
Affiliations

Affiliations

  • 1 The Key Laboratory of Neural and Vascular Biology, Ministry of Education, The Key Laboratory of Vascular Biology of Hebei Province, Department of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, China.
  • 2 The Key Laboratory of Neural and Vascular Biology, Ministry of Education, The Key Laboratory of Vascular Biology of Hebei Province, Department of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, China; Institute of Neuroscience, College of Medicine, Xiamen University, Xiamen, Fujian, 361102, China.
  • 3 State Key Laboratory Breeding Base-Hebei Key Laboratory of Molecular Chemistry for Drug, Hebei Collaborative Innovation Centre of New Drug Creation, College of Chemistry and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang, 050018, China. Electronic address: yidong.liu@hebust.edu.cn.
  • 4 The Key Laboratory of Neural and Vascular Biology, Ministry of Education, The Key Laboratory of Vascular Biology of Hebei Province, Department of Neurobiology, Hebei Medical University, Shijiazhuang, 050017, China. Electronic address: zhangfan86@hebmu.edu.cn.
PMID: 40532787 DOI: 10.1016/j.neuropharm.2025.110565
Abstract

Inhibition of KCNQ-encoded voltage-gated potassium Kv7/M channel function represents an attractive therapeutic strategy for Parkinson's disease (PD). Racecadotril (acetorphan), an inhibitor of the enzyme neutral endopeptidase, has been clinically used to treat acute diarrhea. In this study, we investigated the effects of racecadotril through recording the Kv7.1-Kv7.5 channel currents expressed in CHO cell lines. Our results demonstrate that racecadotril inhibited Kv7.2/Kv7.3 currents in a concentration-dependent manner, with an IC50 value of 7.1 ± 0.83 μM. Racecadotril significantly right-shifted the voltage-dependent activation curve of the Kv7.2/Kv7.3 channels. Additionally, it potently inhibited Kv7.1, Kv7.2, Kv7.4, and Kv7.5 channels, while exerting weak inhibitory effects on the Kv7.3 channel. Notably, we found that thiorphan, the in vivo metabolite of racecadotril, also significantly inhibits Kv7.2, Kv7.4, and Kv7.5 channel currents; however, it does not inhibit the Kv7.2 (W236L), Kv7.4 (W242A) or Kv7.5 (W270A) mutants. Moreover, intraperitoneal administration of racecadotril in 8-week-old male C57BL/6 mice inhibited MPTP-induced motor dysfunction in this PD model, an effect that was blocked by the Kv7 channel opener retigabine (RTG). Taken together, our findings indicate that racecadotril is a potent inhibitor of Kv7.1, Kv7.2, Kv7.4 and Kv7.5 channels, which effectively ameliorates symptoms of PD in rodents.

Keywords

Kv7/M channel; Parkinson's disease; Racecadotril; Thiorphan.

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